欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/1170/002
药品名称
Metformin 850 mg
活性成分
Metformin hydrochloride 500.0 mg
剂型
Film-coated tablet
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327 AH Almere
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
United Kingdom (Northern Ireland) (XI)
France (FR)
Spain (ES)
Sweden (SE)
Norway (NO)
Finland (FI)
Poland (PL)
Czechia (CZ)
许可日期
2008/11/13
最近更新日期
2025/01/29
药物ATC编码
A10BA02 metformin
申请类型
TypeLevel1：
Abridged
TypeLevel2：
Additional Strength/Form
TypeLevel3：
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final Product Information
|
1_3_1 spc_label_pl _ common_outer _ 4_676_Clean
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl _ 9_543
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc _ 9_018_Clean
Date of last change:2024/09/06
Final Labelling
|
common_Label_clean
Date of last change:2024/09/06
Final PL
|
common_pl_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase